# RANOLAZINE

NDC: 77771-424
Generic name: RANOLAZINE
Labeler / Manufacturer: Radha Pharmaceuticals, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250630

FDA application: ANDA211829

## Active ingredients

- RANOLAZINE: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"77771-424"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=77771-424
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=38d2833d-44b8-8d46-e063-6394a90a74d8